Canonical Allele Identifier: CA403982924

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463123T>G (hg19) ; chr19:g.10352447T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352447T>G , CM000681.2:g.10352447T>G	GRCh38
NC_000019.9:g.10463123T>G , CM000681.1:g.10463123T>G	GRCh37
NC_000019.8:g.10324123T>G	NCBI36
NG_007872.1:g.33126A>C , LRG_121:g.33126A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1654A>C	ENSP00000514307.1:n.*1654A>C
ENST00000525976.6:c.3305A>C	ENSP00000434831.2:p.Gln1102Pro
ENST00000527481.3:c.*75A>C	ENSP00000466340.2:n.*75A>C
ENST00000529370.6:n.4681A>C
ENST00000529739.2:n.4114A>C
ENST00000530829.2:c.*2856A>C	ENSP00000436826.2:n.*2856A>C
ENST00000531836.6:c.3305A>C	ENSP00000436175.2:p.Gln1102Pro
ENST00000533334.2:c.*1242+479A>C	ENSP00000432320.2:n.*1242+479A>C
ENST00000534228.2:n.5054+479A>C
ENST00000699354.1:n.1407A>C
ENST00000699355.1:c.*2805A>C	ENSP00000514328.1:n.*2805A>C
ENST00000699356.1:n.4114A>C
ENST00000699357.1:n.5159A>C
ENST00000699358.1:c.3200+479A>C	ENSP00000514329.1:n.3200+479A>C
ENST00000699359.1:c.479A>C
ENST00000699360.1:c.3263A>C	ENSP00000514331.1:p.Gln1088Pro
ENST00000699361.1:n.339A>C
ENST00000699362.1:c.201A>C	ENSP00000514332.1:n.201A>C
ENST00000699363.1:c.201A>C	ENSP00000514333.1:n.201A>C
ENST00000699364.1:n.305A>C
ENST00000699365.1:c.374A>C	ENSP00000514334.1:p.Gln125Pro
ENST00000699366.1:n.111+1367A>C
ENST00000699367.1:n.112-1285A>C
ENST00000699368.1:c.792A>C	ENSP00000514335.1:n.792A>C
ENST00000525621.6:c.3305A>C MANE Select	ENSP00000431885.1:p.Gln1102Pro
ENST00000264818.10:c.3305A>C	ENSP00000264818.6:p.Gln1102Pro
ENST00000524462.5:c.2750A>C	ENSP00000433203.1:p.Gln917Pro
ENST00000525621.5:c.3305A>C	ENSP00000431885.1:p.Gln1102Pro
ENST00000525976.5:c.46A>C
ENST00000527481.2:c.482A>C
ENST00000529422.1:n.116+575A>C
ENST00000529739.1:c.374A>C	ENSP00000436155.1:p.Gln125Pro
ENST00000530220.1:n.331+479A>C
ENST00000530560.5:c.338-1479A>C	ENSP00000465291.1:n.338-1479A>C
ENST00000592137.1:n.459A>C
NM_003331.4:c.3305A>C , LRG_121t1:c.3305A>C	NP_003322.3:p.Gln1102Pro
XM_011528245.1:c.3305A>C	XP_011526547.1:p.Gln1102Pro
XM_011528246.1:c.3008A>C	XP_011526548.1:p.Gln1003Pro
XM_011528247.1:c.3008A>C	XP_011526549.1:p.Gln1003Pro
XM_011528248.1:c.3200+479A>C	XP_011526550.1:n.3200+479A>C
XM_011528249.1:c.1979A>C	XP_011526551.1:p.Gln660Pro
XM_011528251.1:c.1562A>C	XP_011526553.1:p.Gln521Pro
XM_011528246.3:c.3008A>C	XP_011526548.1:p.Gln1003Pro
XM_011528249.2:c.1979A>C	XP_011526551.1:p.Gln660Pro
XR_001753750.1:n.3357+479A>C
XR_001753751.1:n.3857A>C
XR_002958353.1:n.4783A>C
NM_003331.5:c.3305A>C MANE Select	NP_003322.3:p.Gln1102Pro
NM_001385197.1:c.3305A>C	NP_001372126.1:p.Gln1102Pro
NM_001385198.1:c.3168+511A>C	NP_001372127.1:n.3168+511A>C
NM_001385199.1:c.3119A>C	NP_001372128.1:p.Gln1040Pro
NM_001385200.1:c.3302A>C	NP_001372129.1:p.Gln1101Pro
NM_001385201.1:c.3107A>C	NP_001372130.1:p.Gln1036Pro
NM_001385202.1:c.3221A>C	NP_001372131.1:p.Gln1074Pro
NM_001385203.1:c.3386A>C	NP_001372132.1:p.Gln1129Pro
NM_001385204.1:c.3515A>C	NP_001372133.1:p.Gln1172Pro
NM_001385205.1:c.3215A>C	NP_001372134.1:p.Gln1072Pro
NM_001385206.1:c.3179A>C	NP_001372135.1:p.Gln1060Pro
NM_001385207.1:c.3287A>C	NP_001372136.1:p.Gln1096Pro